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Hydrazine hydrate (1:1) → HCID 13957274, 화합물

HRID 2118664
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HRID 2118664 반응식
[C:1]1([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[C:2]([O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:14]2C(=O)C3=CC=CC=C3C2=O)=[CH:3][CH:4]=[CH:5][CH:6]=1.O.NN>C(O)C>[NH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][O:7][C:2]1[C:1]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 20192907HCID 20192907, 화합물

생성물 1

HCID 13957274HCID 13957274, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of N-[6-(2-biphenyloxy)hexyl]phthalimide (15.1 g), ethanol (400 ml) and hydrazine hydrate (30 ml) was heated at reflux for 4 hours, cooled to room temperature, filtered, and evaporated to dryness. The material that remained was stirred with dichloromethane (500 ml), filtered and evaporated to yield 1-amino-6-(2-biphenyloxy) as an oil, which was converted to the hydrochloride salt, (m.p. 86°-88° CC.) according to the method of Example IV.

후처리

temperature
was heated
  • temperatureat reflux for 4 hours
  • filtrationfiltered
  • customevaporated to dryness
  • filtrationfiltered
  • customevaporated
  • customto yield 1-amino-6-(2-biphenyloxy) as an oil, which
  • 출처 및 근거

    ORD 기록
    ord-12e0d08ed9044947b8c997b6eab86503
    출처 데이터셋
    uspto-grants-1987_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04680300

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